896-06-0

Basic information

• Product Name: 1,4-Benzenediamine, N,N-dimethyl-N'-[(4-nitrophenyl)methylene]-
• CAS NO: 896-06-0
• Molecular Formula: C15H15N3O2
• Molecular Weight: 269.303
• Mol File: 896-06-0.mol
• Article Data: 5

Chemical Properties

• CAS DataBase Reference: 1,4-Benzenediamine, N,N-dimethyl-N'-[(4-nitrophenyl)methylene]-(CAS DataBase Reference)
• NIST Chemistry Reference: 1,4-Benzenediamine, N,N-dimethyl-N'-[(4-nitrophenyl)methylene]-(896-06-0)
• EPA Substance Registry System: 1,4-Benzenediamine, N,N-dimethyl-N'-[(4-nitrophenyl)methylene]-(896-06-0)

Safety Data

• Hazardous Substances Data: 896-06-0(Hazardous Substances Data)

Usage

Color

Yellow crystalline substance
The compound appears as yellow crystals.

Melting point

119-121°C
The temperature range at which the compound transitions from a solid to a liquid state.

Solubility

Sparingly soluble in water
The compound does not dissolve easily in water.

Functional group

Nitrobenzene
The presence of a nitrobenzene functional group gives the molecule unique chemical properties and reactivity.

Applications

Dyes and pigments production
The compound is used in the manufacturing of dyes and pigments, such as hair dyes and textile dyes.

Field of interest

Organic chemistry
The compound is of interest in the field of organic chemistry due to its unique chemical properties and potential applications.

Industrial uses

Various applications
The compound has a range of industrial applications beyond dyes and pigments production.

Upstream product

• 42344-05-8 4-nitroso-N,N-dimethylaniline hydrochloride 
• 555-16-8 4-nitrobenzaldehdye 
• 83772-59-2 4-<4-benzylidene>-4'-N,N-dimethylaminoaniline 
• 10050-89-2 4-dimethylamino-4'-(N,N-dimethylamino)benzylideneaniline 
• 99-98-9 4-amino-N,N-dimethylaniline 

Downstream Products

• 111536-95-9 3-phenyl-4-(p-N,N-dimethylaminophenyl)-5-(p-nitrophenyl)-4,5-dihydro-1,2,4-oxadiazol 

Relevant articles and documents

Observation of the complex spectra for the supramolecular system involving silver nanoparticles-biaryl Schiff bases containing the nitro group

A series of biaryl Schiff bases containing the nitro groups, 4-XArCH═NArNO2-4′ (XBANO2-4′) and 4-NO2ArCH═NArY-4′ (4-NO2BAY), were synthesized. Also, the fish sperm DNA (fsDNA) and silver nanoparticles (AgNPs) solutions were prepared. By mixing these compounds with fsDNA or AgNPs solution and determining the ultraviolet absorption spectra of the mixture solutions, an interesting phenomenon was found: a new absorption peak λmax,lim appeared in the (XBANO2-4′)-AgNPs solution, which was longer than the wavelength of λmax of XBANO2-4′ solution. The new absorption peak in the (XBANO2-4′)-AgNPs solution was the complex spectrum originating from the electron transfer between XBANO2-4′ and AgNPs. Whereas this phenomenon was not observed in the (4-NO2BAY)-AgNPs solutions, a quantitative correlation analysis was carried out with the measured spectral data, and the results show that the wave number νmax,lim of the λmax,lim is mainly affected by the excited-state substituent constant (Formula presented.) rather than the ground Hammett constant σ of the X group. The redshift magnitude Δνmax,WSL, namely, Δνmax,WSL = (1/λmax) ? (1/λmax,lim), of the wavelength λmax,lim is related to the highest occupied molecular orbital and lowest unoccupied molecular orbital of XBANO2-4′. The discovery of this new phenomenon is helpful to understanding the interaction between AgNPs-organic compound supramolecular systems.

ELECTRONIC ABSORPTION SPECTRA OF AROMATIC SCHIFF BASES. PART III. p-PHENYLENEDIAMINE DERIVATIVES

The effect of para substituents in the benzylidene-p-dimethylaminoaniline and dibenzylidene-p-phenylenediamine molecules on their UV-VIS spectra has been studied.A linear relationship has been found between position of the most long-wavelength absorption

SEMICONDUCTIVITY OF ORGANIC SUBSTANCES-15

Part 15 treats compounds related to stilbene. Dark conductivity in diphenylbutadiene and four analogs of stilbene has been examined. The compounds were chosen to reveal the possible effects of a donor and an acceptor group attached to opposite ends of the